柠檬酸溶液稳定性的研究与开发

Q3 Pharmacology, Toxicology and Pharmaceutics
T. A. Bitkina, A. V. Basevich
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引用次数: 1

摘要

介绍本文介绍了基于商品酸物质的溶液的发展。在“设计质量”概念的框架内,对所研究的成分在储存过程中影响其稳定性的标准进行了评估。确定了柠檬酸溶液的最佳组成。目标该研究的目的是开发基于商品酸物质的解决方案,并确定最稳定的执行变体。材料和方法。使用实验室pH计PB-11-P11(SARTORIUS,德国)和液相/离子色谱仪“Stayer”(“Akvilon”JSC,俄罗斯)对柠檬酸溶液进行了研究。结果和讨论。这项研究使人们有可能根据商品酸物质确定溶液中最稳定的成分,并建立其稳定性标准的最佳指标。研究发现,在4.0~6.0的pH范围内,柠檬酸溶液是最稳定的。同时,无论所研究的彗星酸中和方法如何,溶液在25 mg/ml或更高的浓度下都是不稳定的。结论作为研究的结果,确定了基于商品酸物质的溶液的最佳组成。对可增加comenic酸在水性溶剂中溶解度的赋形剂进行了比较分析。建立了所研究溶液的稳定性标准,并确定了其确保所开发药物稳定性的值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and study of the stability of comenic acid solutions
Introduction. The article presents the development of solutions based on the comenic acid substance. The criteria of the studied compositions that affect their stability during storage are evaluated within the framework of the Quality-by-Design concept. The optimal compositions of comenic acid solutions have been established.Aim. The purpose of the study is to develop solutions based on the comenic acid substance and determine the most stable variants of execution.Materials and methods. The study of comenic acid solutions was carried out by using a laboratory pH meter PB-11-P11 (SARTORIUS, Germany) and a liquid/ion chromatograph "Stayer" ("Akvilon" JSC, Russia).Results and discussion. The study made it possible to determine the most stable compositions of solutions based on the comenic acid substance and to establish optimal indicators of their stability criteria. It was found that solutions of comenic acid are the most stable in the pH range: from 4.0 to 6.0. At the same time, regardless of the studied methods of neutralization of comenic acid, solutions are unstable at concentrations of 25 mg/ml or more.Conclusion. As a result of the study, the optimal compositions of solutions based on the comenic acid substance were determined. A comparative analysis of excipients that increase the solubility of comenic acid in aqueous solvents is performed. The stability criteria of the studied solutions are established and their values for ensuring the stability of the developed drug are determined.
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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